Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C229/00—Compounds containing amino and carboxyl groups bound to the same carbon skeleton
  • C07C229/02—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton
  • C07C229/34—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton containing six-membered aromatic rings
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P25/00—Drugs for disorders of the nervous system
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P25/00—Drugs for disorders of the nervous system
  • A61P25/04—Centrally acting analgesics, e.g. opioids
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P25/00—Drugs for disorders of the nervous system
  • A61P25/06—Antimigraine agents
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P25/00—Drugs for disorders of the nervous system
  • A61P25/08—Antiepileptics; Anticonvulsants
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P25/00—Drugs for disorders of the nervous system
  • A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P25/00—Drugs for disorders of the nervous system
  • A61P25/20—Hypnotics; Sedatives
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P25/00—Drugs for disorders of the nervous system
  • A61P25/22—Anxiolytics
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P25/00—Drugs for disorders of the nervous system
  • A61P25/24—Antidepressants
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P25/00—Drugs for disorders of the nervous system
  • A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P25/00—Drugs for disorders of the nervous system
  • A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P25/00—Drugs for disorders of the nervous system
  • A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
  • A61P25/36—Opioid-abuse
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C225/00—Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones
  • C07C225/02—Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones having amino groups bound to acyclic carbon atoms of the carbon skeleton
  • C07C225/14—Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones having amino groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being unsaturated
  • C07C225/16—Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones having amino groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being unsaturated and containing six-membered aromatic rings
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
  • C07C237/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton
  • C07C237/20—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton containing six-membered aromatic rings
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C243/00—Compounds containing chains of nitrogen atoms singly-bound to each other, e.g. hydrazines, triazanes
  • C07C243/10—Hydrazines
  • C07C243/22—Hydrazines having nitrogen atoms of hydrazine groups bound to carbon atoms of six-membered aromatic rings
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C255/00—Carboxylic acid nitriles
  • C07C255/49—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
  • C07C255/58—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing cyano groups and singly-bound nitrogen atoms, not being further bound to other hetero atoms, bound to the carbon skeleton
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
  • C07D241/02—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
  • C07D241/10—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
  • C07D241/14—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
  • C07D241/20—Nitrogen atoms
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
  • C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
  • C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
  • C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
  • C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
  • C07D261/10—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
  • C07D261/14—Nitrogen atoms
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
  • C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
  • C07D317/44—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems
  • C07D317/46—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with one six-membered ring
  • C07D317/48—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring
  • C07D317/62—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to atoms of the carbocyclic ring
  • C07D317/66—Nitrogen atoms not forming part of a nitro radical
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C2601/00—Systems containing only non-condensed rings
  • C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
  • C07C2601/14—The ring being saturated

Definitions

• GABA controls brain excitability by exerting inhibitory functions on neuronal membranes by altering their permeability to specific ions. Binding of GABA to the GABA A -type (GABA A ) receptor increases the permeability of neuronal membranes to chloride ions (Cf)- i most neurons the relative Cl " ion concentration is greater outside than inside the membrane. Thus, selective permeability to Cl " initiated by GABA binding forces Cl " into the cell. The majority of fast inhibitory synaptic transmission is a result of GABA binding to the GABA A receptors. GABA A receptors are ubiquitously expressed throughout the CNS with almost all neurons staining for their presence.
• the GABA A receptor is a hetero-pentameric protein structure of the nicotinic acetylcholine receptor superfamily.
• Native GABAA receptors are formed from at least 19 related subunits. The subunits are grouped into ⁇ , ⁇ , ⁇ , ⁇ , ⁇ , and p families.
• the most prevalent combination of GABA A receptors is a stoichiometric combination of the 2 x ⁇ , 2 x ⁇ , and 1 x ⁇ subunits, with the remaining subunits relegated to substituting for the ⁇ subunit during specific development expression or in highly specific brain region localization.
• the adult brain predominately expresses the ⁇ 2 ⁇ 2 subunit combination (60%) with the 2 ⁇ 3 ⁇ 2 and ⁇ 3 ⁇ n ⁇ 2 subunits comprising the majority (35%) of the remaining receptors.
• the relative effects of GABA are influenced by the GABA A receptor subunit expressed in a specific brain region or neuronal circuit.
• the neurophysiological effects of GABA result from a conformational change that occurs when GABA binds to the GABA A receptor.
• the GAB A A receptor and the associated ion channel complex (GRC) recognize many compounds that allosterically enhance the ability of GABA to bind to the GAB A A receptor.
• the allosteric modulators have distinct sites on the GRC.
• GRC GABA receptor pharmacology
• neuroactive steroids are non-hormonal steroids that bind and functionally modulate the GRC.
• the current role of neuroactive steroids in GABAA receptor pharmacology is supported by overwhelming evidence. Electrophysiological and biochemical techniques have confirmed the capacity of neuroactive steroids to allosterically modulate the GRC through a unique site of action. Experimentally, neuroactive steroids exhibit a pharmacological profile similar, but not identical, to the benzodiazepines.
• GABA and drugs that act like GABA or facilitate the effects of GABA e.g., the therapeutically useful barbiturates and benzodiazepines (BZs) such as Valium
• BZs benzodiazepines
• the present invention is related to the discovery that certain substituted enaminones represented by Formula I act as enhancers of GABA-facilitated Cl " flux mediated through the GABA A receptor complex (GRC).
• GAC GABA A receptor complex
• the invention is related to treating disorders responsive to enhancement of GABA action on GABA receptors in a mammal by administering an effective amount of a compound of Formula I as described herein.
• the compounds of the present invention being ligands for GABA A receptors, are therefore of use in the treatment and/or prevention of a variety of disorders of the central nervous system (CNS).
• the compounds are useful for the treatment and/or prevention of disorders of the CNS involving neuronal hyperexcitability.
• Such disorders include but are not limited to anxiety disorders, such as panic disorder with or without agoraphobia, agoraphobia without history of panic disorder, animal and other phobias including social phobias, obsessive- compulsive disorder, stress disorders including post-traumatic and acute stress disorder, and generalized or substance-induced anxiety disorder, neuroses, convulsions, migraine, and depressive or bipolar disorders, for example single-episode or recurrent major depressive disorder, dysthymic disorder, bipolar I and bipolar II manic disorders, and cyclothymic disorder.
• Another aspect of the present invention is directed to the use of the compounds of Formula I as enhancers of GABA-facilitated Cl " flux mediated through the GABA A receptor complex.
• an aspect of the present invention is to provide a pharmaceutical composition useful for treating disorders responsive to the enhancement GABA-facilitated Cl " flux mediated through the GRC, containing an effective amount of a compound of Formula I in a mixture with one or more pharmaceutically acceptable carriers or diluents.
• Compounds useful in the present invention have not been heretofor reported.
• the present invention is also directed to novel substituted enaminones having the stracture of Formula I.
• the compound of Formula I or pharmaceutically acceptable salts thereof act by binding to a site other than a site that binds [ H]-flunitrazepam, barbiturates, loreclezole, [ H]-muscimol or 3 ⁇ ,20 ⁇ -pregnanediol, thereby altering chloride conductance through the GABA A receptor complex in a therapeutically usefully fashion.
• the present invention is directed to 3 H, 35 S, 3 ⁇ Cl, 14 C and 125 I radiolabeled compounds of Formula I and their use as radioligands for their binding site on the GRC.
• Figure 2 Dose response of 5 ⁇ -pregnan-3 ⁇ , 20 ⁇ -diol in the absence and presence of 30 nM ethyl 2-chloro- ⁇ -[[(4-ethynylphenyl)amino]methylene]- ⁇ -oxo-benzenepropionate or 100 nM ⁇ -[[(4-ethynylphenyl)amino]methylene]-2-chloro- ⁇ -oxo-N-propyl-benzenepropanamide on 2 nM [ 35 S]TBPS binding in rat cortex.
• Figure 3 Dose response of ethyl 2-chloro- ⁇ -[[(4-ethynylphenyl)amino]methylene]- ⁇ - oxo-benzenepropionate, ⁇ -[[(4-ethynylphenyl)amino]methylene]-2-chloro- ⁇ -oxo-N-propyl- benzenepropanamide, and ⁇ -aminobutyric acid on 5 nM [ Ffjmuscimol binding in rat cortex.
• Figure 4 Dose response of loreclezole in the presence and absence of 300 nM ethyl 2- chloro- ⁇ -[[(4-ethynylphenyl)amino]methylene]- ⁇ -oxo-benzenepropionate on 0.2 nM [ 3 H]flunitrazepam binding in rat cortex.
• Figure 5 Dose response of pentobarbital in the presence and absence of 300 nM ethyl 2- chloro- ⁇ -[[(4-ethynylphenyl)amino]methylene]- ⁇ -oxo-benzenepropionate on 0.2 nM [ 3 H]flunitrazepam binding in rat cortex.
• substituted enaminones represented by Formula I: or a pharmaceutically acceptable salt, prodrug or solvate thereof, wherein: Ri is selected from the group consisting of aryl, heteroaryl, aralkyl and R ⁇ 6 R ⁇ N-, each unsubstituted or substituted; R 2 is selected from the group consisting of hydrogen and unsubstituted or substituted Ci- l oalkyl; R 3 is selected from the group consisting of fluoro, chloro, bromo, iodo, Ci.inalkoxy, nitro, haloCi.ioalkyl, perhaloC 1-10 alkyl and unsubstituted or substituted Ci-ioalkyl; each R 4 is independently selected from the group consisting of halogen, nitro, Ci-ioalkyl, C 2- ⁇ 0 alkenyl, C 2- ⁇ oalkynyl, C ⁇ . ⁇ 0 alkoxy,
• Ri is selected from the group consisting of aryl, heteroaryl, aralkyl and R ⁇ 6 R ⁇ 7 N-, each unsubstituted or substituted
• R 2 is selected from the group consisting of hydrogen and unsubstituted or substituted C ⁇ _ loalkyl
• R 3 is selected from the group consisting of hydrogen, halo, haloCi-ioalkyl, perhaloCi.
• each R 4 is independently selected from the group consisting of halogen, nitro, Ci.ioalkyl, C 2- ⁇ oalkenyl, C 2-1 oalkynyl, Ci-ioalkoxy, aralkyl, aryl, heteroaryl, cycloalkyl and heterocycloalkyl, each unsubstituted or substituted, or wherein R 3 and an adjacent R 4 together form a fused unsubstituted or substituted, or wherein R 3 and an adjacent R 4 together form a fused unsubstit
• Ri is selected from the group consisting of aryl, heteroaryl, aralkyl and R 16 R 17 N-, each unsubstituted or substituted
• R 2 is selected from the group consisting of hydrogen and unsubstituted or substituted Ci- ioalkyl
• R 3 is selected from the group consisting of hydrogen, halo, haloCi-ioalkyl, perhaloCi.
• each R_j is independently selected from the group consisting of hydrogen, halo, nitro, perhaloCi.ioalkyl, amino, cyano, nitro, hydroxy, thio, C ⁇ -2 oalkyl, C 2- ⁇ 0 alkenyl, C 2- ⁇ oalkynyl, cycloalkyl, heterocycloalkyl, aryl, aralkyl, heteroaryl, Ci-ioalkoxy, aryloxy, heteroaryloxy, carbonyl group, sulfonyl group, sulfmyl group, imino group, each unsusbtituted or substituted; each R_j is independently selected from the group consisting of hydrogen, halo, nitro, perhaloCi.ioalkyl, amino, cyano, nitro, hydroxy, thio, C ⁇ -2 oalkyl, C 2- ⁇ 0 alkenyl, C 2- ⁇ oalkynyl, cycloalky
• R 5 is C ⁇ - ⁇ oalkylamino
• the stereochemistry of the enaminone is such that the -NHRi is syn with the -COR 5 group as shown in Formula lb below.
• the group -NHC ⁇ - oalkyl is selected from the group consisting of -NHC 2 . ⁇ oalkyl.
• the group C 2 _ ⁇ oalkyl is wopropyl, propyl, sec-butyl, tert-butyl, 2 -methyl- 1 -butyl and 3 -methyl- 1 -butyl.
• R 2 is selected from the group consisting of hydrogen, methyl and ethyl
• R 3 is selected from the group consisting of hydrogen, halo, haloCi-ioalkyl, perhaloCi- l oalkyl, amino, cyano, nitro, hydroxy, thio, C ⁇ -2 oalkyl, C 2- ⁇ oalkenyl, C - ⁇ oalkynyl, cycloalkyl, heterocycloalkyl, aryl, aralkyl, heteroaryl, Ci-ioalkoxy, aryloxy, heteroaryloxy, carbonyl group, sulfonyl group, sulfmyl group, imino group, each unsusbtituted or substituted; each R4 is independently selected from the group consisting of hydrogen, halo, nitro, haloCi-ioalkyl, perhaloCi-i
• R 6 , R , Rs, R 9 and Rio are each independently selected from the group consisting of hydrogen, halo, Ci-ioalkyl, C 2- ⁇ oalkynyl, Ci-ioalkoxy, aralkyl, cycloalkyl, arylCi-ioalkyl and heteroarylCi-ioalkyl; or
• Ri is selected from the group consisting of aryl, heteroaryl, aralkyl and R ⁇ 6 R ⁇ N-, each unsubstituted or substituted;
• R is selected from the group consisting of hydrogen and unsubstituted or substituted Ci-ioalkyl;
• R 5 is selected from the group consisting of Ci-ioalkyl, Ci-ioalkoxy, -NH 2 , Ci-ioalkylamino, di(C ⁇ - ⁇ o)alkylamino and aryl, each unsubstituted or substituted;
• R ⁇ 6 and R 1 are each independently C 3- ⁇ 2 cycloalkyl, aryl, heteroaryl, Ci-ioalkyl, each unsubstituted or substituted, or R 16 and Rj 7 together with the nitrogen atom to which they are attached form an unsusbtituted or substituted 4, 5, or 6 membered ring;
• R ⁇ 9 and R are each independently C 3- ⁇ 2 cycloal
• a compound comprising the Formula III: or a pharmaceutically acceptable salt, prodrug or solvate thereof, wherein: R 2 is selected from the group consisting of hydrogen and unsubstituted or substituted Ci. l oalkyl; R 3 is selected from the group consisting of fluoro, chloro, bromo, iodo, Ci-ioalkoxy, nitro, haloCi-ioalkyl, perhaloCi-ioalkyl and unsubstituted or substituted Ci-ioalkyl; each 1 ⁇ is independently selected from the group consisting of halogen, nitro, Ci-ioalkyl,
• R 5 is selected from the group consisting of Ci-ioalkyl, Ci-ioalkoxy, -NH 2 ,
• R 6 , R 7 , Rs, R 9 and Rio are each independently selected from the group consisting of hydrogen, halo, Ci-ioalkyl, C 2 - ⁇ oalkynyl, Ci-ioalkoxy, aralkyl, cycloalkyl, arylCi-ioalkyl and heteroarylCi-ioalkyl; or R 6 and R 7 , or R and R 8 , or R 8 and R , or R 9 and R ⁇ are taken together with the carbon atoms to which they are attached to form an unsubstituted or substituted fused 5 or 6 membered saturated, partially unsaturated ring, aryl or heteroaryl; and m is 0, 1, 2, 3 or 4.
• a compound comprising the Formula IV:
• R 2 is selected from the group consisting of hydrogen and unsubstituted or substituted Ci- l oalkyl
• R 3 is selected from the group consisting of fluoro, chloro, bromo, iodo, Ci-ioalkoxy, nitro, haloCi-ioalkyl, perhaloCi-ioalkyl and unsubstituted or substituted Ci-ioalkyl
• each R 4 . is independently selected from the group consisting of halogen, nitro, Ci-ioalkyl
• R 5 is selected from the group consisting of Ci-ioalkyl, Ci-ioalkoxy, -NH , C ⁇ - ⁇ oalkylamino, di(C 1- ⁇ o)alkylamino and aryl, each unsubstituted or substituted;
• R 6 , R 7 , R 8 , R 9 and Rio are each independently selected from the group consisting of hydrogen, halo, Ci-ioalkyl, C 2- ⁇ oalkynyl, Ci-ioalkoxy, aralkyl, cycloalkyl, arylCi
• R 2 is selected from the group consisting of hydrogen, methyl and ethyl
• R 3 is selected from the group consisting of hydrogen, halo, haloCi-ioalkyl, perhaloCi- l oalkyl, amino, cyano, nitro, hydroxy, thio, C ⁇ -2 oalkyl, C 2- ⁇ oalkenyl, C 2- ⁇ oalkynyl, cycloalkyl, heterocycloalkyl, aryl, aralkyl, heteroaryl, Ci-ioalkoxy, aryloxy, heteroaryloxy, carbonyl group, sulfonyl group, sulfmyl group, imino group, each unsusbtituted or substituted; each R 4 is independently selected from the group consisting of halogen, nitro, Ci-ioalkyl,
• R 5 is selected from the group consisting of Ci-ioalkyl, Ci-ioalkoxy, -NH , Ci-ioalkylamino, di(C ⁇ - ⁇ o)alkylamino and aryl, each unsubstituted or substituted;
• R 6 , R 7 , Rs, R 9 and Rio are each independently selected from the group consisting of hydrogen, halo, Ci-ioalkyl, C 2- ⁇ oalkynyl, Ci-ioalkoxy, aralkyl, cycloalkyl, arylCi
• R is selected from the group consisting of hydrogen, halo, haloCi-ioalkyl, perhaloCi- l oalkyl, amino, cyano, nitro, hydroxy, thio, C ⁇ - oalkyl, C 2- ⁇ oalkenyl, C 2 .
• each R 4 is independently selected from the group consisting of hydrogen, halo, haloCi. l oalkyl, perhaloCi-ioalkyl, amino, cyano, nitro, hydroxy, thio, C ⁇ -2 oalkyI, C - ⁇ oa ⁇ kenyl,
• R 2 is selected from the group consisting of hydrogen and unsubstituted or substituted Ci l oalkyl
• R 3 is selected from the group consisting of hydrogen, halo, haloCi-ioalkyl, perhaloCi. l oalkyl, amino, cyano, nitro, hydroxy, thio, C 1 .
• each i is independently selected from the group consisting of hydrogen, halo, haloCi- l oalkyl, perhaloCi-ioalkyl, amino, cyano, nitro, hydroxy, thio, C ⁇ -2 oalkyl, C 2- ⁇ oalkenyl, C 2- ⁇ oalkynyl, cycloalkyl, heterocycloalkyl, aryl, aralkyl, heteroaryl, Ci-ioalkoxy, aryloxy, heteroaryloxy, carbonyl group, sulfonyl group, sulfinyl group, imino group, each unsusbtituted or substituted; each i is independently selected from the group consisting of hydrogen, halo, haloCi- l oalkyl, perhaloCi-ioalkyl, amino, cyano, nitro, hydroxy, thio, C ⁇ -2 oalkyl, C 2- ⁇ oalken
• Ri is selected from the group consisting of aryl, heteroaryl, aralkyl and R ⁇ 6 R ⁇ N-, each unsubstituted or substituted
• R 2 is selected from the group consisting of hydrogen and unsubstituted or substituted Ci- l oalkyl
• R 3 is selected from the group consisting of hydrogen, halo, haloCi-ioalkyl, perhaloC].
• each R 4 is independently selected from the group consisting of halogen, nitro, Ci-ioalkyl, C 2 - ⁇ oalkynyl, Ci-ioalkoxy, aralkyl, aryl, heteroaryl, cycloalkyl and heterocycloalkyl, each unsubstituted or substituted, or wherem R 3 and an adjacent R 4 together form a fused unsubstituted or substituted 5
• ⁇ o)alkyl, amino, hydroxyl, thio and Ci-ioalkoxy, and m and p are each independently 0, 1, 2, 3 or 4.
• R 8 is selected from the group consisting of C ⁇ _ l oalkyl, halogen, and Ci-ioalkoxy; and R 6 , R 7 , R 9 and Rio are hydrogen.
• R 3 is selected from the group consisting of methyl, trifluoromethyl and chloro; and m is 0.
• a pharmaceutical composition comprising the' compound of Formula I:
• Ri is selected from the group consisting of aryl, heteroaryl, aralkyl and R 16 R 17 N-, each unsubstituted or substituted; R is selected from the group consisting of hydrogen and unsubstituted or substituted C ⁇ .
• compositions of the above compounds wherein the composition is formulated for oral administration, parentaral, intraavenous, transdennal, sublingual, intramuscular, rectal, intranasal, intraoccular or subcutaneous administration.
• a pharmaceutical composition comprising each of the above compound and a pharmaceutically-acceptable carrier selected from the group consisting of excipients and auxiliaries.
• a method for the treatment of CNS disorders amenable to modulation of the GABA A receptor complex which comprises administering to a patient in need of such treatment a compound of Formula I:
• the CNS disorder is an anxiety disorder.
• the CNS disorder is convulsions.
• the CNS disorder is insomnia.
• the CNS disorder is a major depressive or bipolar disorder.
• the CNS disorder is chronic or acute pain.
• the CNS disorder is a neuroses.
• the CNS disorder is withdrawal-induced convulsions from substance abuse.
• the CNS disorder is a phobia.
• the CNS disorder is a panic disorder.
• the CNS disorder is a generalized anxiety disorder.
• the CNS disorder is an obsessive-compulsive disorder.
• the CNS disorder is a post traumatic and acute stress disorder.
• the CNS disorder is a migraine.
• the CNS disorder is a bipolar manic disorder; or a cognition deficit disorder.
• the CNS disorder is selected from the group consisting of anxiety and stress related disorders, depression and other affective disorders, epilepsy and other seizure disorders, insomnia and related sleep disorders, acute and chronic pain and cough.
• a method for the treatment of disorders related to learning and memory comprising the steps of administering to a patient in need of such a treatment a compound of the Formula I above.
• the disorder relating to learning and memory is selected from the group consisting of mild cognitive impairment, age related cognitive decline, senile dementia, Alzheimer's disease, sleep disorders involving reduced wakefulness.
• the sleep disorder involving reduced wakefulness is selected from the group consisting of narcolepsy and idiopathic hypersomnia.
• a method wherein the compound of Formula I or a pharmaceutically acceptable salt thereof acts by binding to a site other than a site that binds [ H]- flunitrazepam, barbiturates, loreclezole, [ 3 H]-muscimol or 3 ,20 ⁇ -pregnanediol, thereby altering chloride conductance through the GABA A receptor complex in a therapeutically usefully fashion.
• a method for the treatment of CNS disorders amenable to modulation of the GABA A receptor complex which comprises administering to a patient in need of such treatment a compound of Formula I.
• the present invention is also related to the discovery that certain substituted enaminones represented by Formulae I- VI act as novel modulators of ⁇ 7 nicotinic acetylcholine receptors (nAChRs).
• the invention is related with treating disorders responsive to enhancement of acetylcholine action on cc7 nAChRs in a mammal by administering an effective amount of a compound of Fonnulae I- VI as described herein.
• the compounds of the present invention being ligands for ⁇ 7 nAChRs, are therefore of use in the treatment and/or prevention of a variety of disorders of the central nervous system.
• Such disorders include neuro degenerative diseases, senile dementias and schizophrenia.
• Another aspect of the present invention is directed to the use of the compounds of Formulae I- VI as enhancers of acetylcholine- facilitated monovalent and divalent cation flux mediated through the ⁇ 7 nAChR.
• an aspect of the present invention is to provide a pharmaceutical composition useful for treating disorders responsive to the enhancement of acetylcholine-facilitated monvalent and divalent cation mediated flux through the nAChR, containing an effective amount of a compound of Formulae I- VI in a mixture with one or more pharmaceutically acceptable carriers or diluents.
• a method for the treatment of CNS disorders amenable to modulation of the nAChR complex which comprises administering to a patient in need of such treatment a compound of Formula I:
• Ri is selected from the group consisting of aryl, heteroaryl, aralkyl and R ⁇ 6 R ⁇ 7 N-, each unsubstituted or substituted;
• R 2 is selected from the group consisting of hydrogen and unsubstituted or substituted Ci.
• R 3 is selected from the group consisting of hydrogen, halo, haloCi-ioalkyl, perhaloCi- loalkyl, amino, cyano, nitro, hydroxy, thio, C ⁇ -2 oalkyl, C 2 - ⁇ oalkenyl, C 2 _ ⁇ oalkynyl, cycloalkyl, heterocycloalkyl, aryl, aralkyl, heteroaryl, Ci-ioalkoxy, aryloxy, heteroaryloxy, carbonyl group, sulfonyl group, sulfmyl group, imino group, each unsusbtituted or substituted; each i is independently selected from the group consisting of hydrogen, halo, haloCi- l oalkyl, perhaloCi-ioalkyl, amino, cyano, nitro, hydroxy, thio, C ⁇ _ 2 oalkyl, C 2 - ⁇ oal
• a method for the treatment of neurodegenerative disorders which comprises administering to a patient in need of such treatment an effective amount of compound of the Formulae I- VI.
• a method for the treatment of senile dementias which comprises administering to a patient in need of such treatment an effective amount of compound of the Formulae I- VI.
• a method for the treatment of schizophrenia which comprises administering to a patient in need of such treatment an effective amount of compound of the Formulae I- VI.
• a method for the treatment of cognition deficit disorders which comprises administering to a patient in need of such treatment an effective amount of compound of the Formulae I- VI.
• a method for the treatment of disorders related to learning and memory such as mild cognitive impainnent, age related cognitive decline, senile dementia, Alzheimer's disease, by inhibition of mono and divalent cation conductance through the site mediating the action of compound of the above Formulae I- VI.
• Compounds of Formulae I- VI include: Ethyl 2-chloro- ⁇ -oxo- ⁇ - [ [ [4-( 1 ,2,3 ,4-tetrahydronaphthyl- 1 -amino)phenyl] amino] - methylenejbenzenepropionate; Ethyl 2-chloro-5-nitro- ⁇ -oxo- ⁇ -[[[4-(l,2,3,4-tetrahydronaphthyl-l-amino)- phenyl]amino]methylene]benzenepropionate; Ethyl 2-chloro- ⁇ -[(cyclohexylamino)methylene]- ⁇ -oxobenzenepropionate;
• the salts of the compounds of Formulae I- VI will be pharmaceutically acceptable salts.
• Other salts may, however, be useful in the preparation of the compounds according to the invention or of their pharmaceutically acceptable salts.
• Suitable pharmaceutically acceptable salts of the compounds of this invention include acid addition salts which may, for example, be formed by mixing a solution of the compound according to the invention with a solution of a pharmaceutically acceptable acid such as hydrochloric acid, sulfuric acid, methanesulfonic acid, fumaric acid, maleic acid, succinic acid, acetic acid, benzoic acid, oxalic acid, citric acid, tartaric acid, or phosphoric acid.
• a pharmaceutically acceptable acid such as hydrochloric acid, sulfuric acid, methanesulfonic acid, fumaric acid, maleic acid, succinic acid, acetic acid, benzoic acid, oxalic acid, citric acid, tartaric acid, or phosphoric acid.
• suitable pharmaceutically acceptable salts thereof may include alkali metal salts, e.g. sodium or potassium salts; alkaline earth metal salts, e.g. calcium or magnesium salts; and salts fonned with suitable organic ligands, e.g. quaternary ammonium salts.
• Standard methods for the preparation of pharmaceutically acceptable salts and their formulations are well known in the art, and are disclosed in various references, including for example, "Remington: The Science and Practice of Pharmacy", A. Gennaro, ed., 20th edition, Lippincott, Williams & Wilkins, Philadelphia, PA.
• the present invention includes within its scope prodrags of the compounds of Formulae
• Fonnulae I- VI that are readily convertible in vivo into the required compound of Formulae I- VI.
• Halogen or “halo” means fluorine, bromine, chlorine and iodine. Useful halogens include fluorine, chlorine, bromine and iodine.
• Alkyl means a straight or branched, saturated or unsaturated aliphatic radical with the number of carbon atoms depicted. An alkyl group may comprise a heteroatom, such as an oxygen, nitrogen or sulfur inserted within or in the chain of the alkyl group.
• Useful alkyl groups include straight chain and branched C 1-2 oalkyl groups. In one aspect, the alkyl group of the present invention comprises the C 5 . oalkyl groups. Typical Cs.
• 2 oalkyl groups include n-penyl, n- hexyl, n-heptyl, n-octyl, n-nonyl, n-decyl, n-undecyl, n-dodecyl, n-tricedyl, n-tetradecyl, n- pentadecyl, n-hexadecyl, n-heptadecyl, n-octadecyl, n-nonadecyl and eicosanyl groups.
• An alkyl group may also be represented with another group, such as an "arylalkyl” group, such as a benzyl group. See below.
• An "aryl” group may be a monocyclic, bicyclic or polycyclic ring system wherein each ring is aromatic, or when fused or connected to one or more rings to form a polycyclic ring system.
• An aryl ring may also be fused with a non-aromatic ring .
• An aryl ring may also contain a heteroatom to form a hetroaryl ring.
• Useful aryl groups are C 6 . ⁇ aryl, especially C 6 - ⁇ oaryl.
• Typical C 6 _i 4 ryl groups include phenyl, naphthyl, anthracyl, indenyl and biphenyl groups.
• An "arylalkyl” or “aralkyl” group includes any of the above-mentioned groups substituted with any of the above-mentioned C 6 - ⁇ oaryl groups.
• a substituted Ci-ioalkyl may also represent an arylalkyl or aralkyl group (or heteroarylalkyl, etc ...) when the Ci-ioalkyl group is substituted with an aryl group.
• Useful arylalkyl groups include benzyl, phenethyl and phenylpropyl.
• a combination group such as a arylalkyl or aralkyl group
• the group is attached at the latter or last represented group.
• an "arylCi-ioalkyl” group such as a benzyl group, for example, is attached at the bond represented here as arylCi-ioalkyl- or benzyl-.
• Useful cycloalkylalkyl groups include any of the above-mentioned C].
• a cycloalkyl group may also comprise one or more heteroatoms in the cyclic group.
• useful cycloalkylalkyl groups include cyclohexylmethyl and cyclopropylmethyl groups.
• Useful halomethyl groups include C ⁇ -2 oalkyl groups substituted with one or more fluorine, chlorine, bromine or iodine atoms, including fluoromethyl, difluoromethyl, trifluoromethyl and 1,1-difluoroethyl groups.
• Perhaloalkyl group include, for example, trifluoromethyl and pentafluoroethyl groups.
• Useful hydroxyalkyl groups include C ⁇ . 2 oalkyl groups substituted by hydroxy group, including hydroxymethyl, 1- and 2-hydroxyethyl and 1-hydroxypropyl groups.
• Useful alkoxy groups include oxygen substitution by one of the C M o lkyl groups described above. Examples of such alkoxy groups include methoxy, ethoxy, propoxy, butoxy, and the like.
• Useful alkylthio groups include sulfur substitution by one of the C 1-2 oalkyl groups described above including for example, thiomethyl, thiobutyl, decyl- and hexadecylthio groups.
• An "amino" group is -NH 2 .
• An alkylamino and dialkylamino groups for example, include the groups -NHR ⁇ and -NR 12 R ⁇ 3 , wherein each R ⁇ 2 and R 13 are independently substituted or unsubstituted C ⁇ -2 oalkyl groups. Example of such groups include -NHMe, -NHEt,
• dialkylaminoalkyl groups include any of the above-mentioned Ci-ioalkyl groups, each substituted or unsubstituted.
• a substituted amino group may include for example, -NHMe, -NHEt, -NHcyclohexyl, -N(Me) 2 and the like, and -NHCOMe, -NHCOEt, -NHCONHMe, and the like.
• alkylthiol groups include any of the above-mentioned Ci-ioalkyl groups substituted by a -SH group.
• Carbonyl means the group -C(O)- that may be attached to another ligand such as an
• carbonyl groups include a carboxy group, aldehyde, acid halide or ketone.
• a carboxy or carboxyl group is -COOH.
• Heterocyclic means a saturated or partially unsaturated 3-7 membered monocyclic or 7-
• 10 membered bicyclic ring system which consists of carbon atoms and from one to four heteroatoms independently selected ' from the group consisting of O, N, and S, wherein the nitrogen and sulfur heteroatoms can be optionally oxidized, the nitrogen can be optionally quatemized, and including any bicyclic group in which any of the above-defined heterocyclic rings is fused to a benzene ring, and wherein the heterocyclic ring can be substituted on carbon or nitrogen if the resulting compound is stable-.
• Examples include, but are not limited to pyn-olidine, piperidine, piperazine, morpholine, quinoline, 1,2,3,4-tetrahydroquinoline, and the like.
• Heteroaryl means wholly unsaturated 5 and 6 membered monocyclic, or 9 and 10 membered bicyclic ring system for example, which consists of carbon atoms and from one to four heteroatoms independently selected from the group consisting of O, N and S, wherein the nitrogen and sulfur heteroatoms can be optionally oxidized, the nitrogen can be optionally quaternized, and including any bicyclic group in which any of the above-defined heterocyclic rings is fused to a benzene ring, and wherein the heterocyclic ring can be substituted on carbon or nitrogen if the resulting compound is stable.
• heteroaryl groups may be unsubstituted or substituted. "Substituted or unsubstituted" means that a group may consist of only hydrogen substituents (unsubstituted) or may further comprise one or more non-hydrogen substituents (substituted) that are not otherwise specified.
• t ⁇ rt-butyl group may be an example of a propyl group that is substituted by a methyl group.
• substituents include, but are not limited to, (C ⁇ - ⁇ o)alkyl, (C 2- ⁇ o)alkylene, amide, amino, aryl, carbamoyl, carbonyl group, cycloalkyl, ester, halo, heteroaryl, oxo, hydroxy or nitro groups, each of which may also be substituted or unsubstituted as valency permits.
• Optional substituents on Ri to R 2 o include any one or more of halo, cyano, nitro, halo(C ⁇ -2 o)alkyl, perhalo(C ⁇ - 2 o)alkyl, aryl, cycloalkyl, C ⁇ .
• a preferred optional substituents include halo, (C ⁇ -6 )alkyl, halo(C ⁇ -6 )alkyl, amino(C ⁇ . 6 )alkyl, C ⁇ -2 ⁇ oalkoxy and amino.
• “Isomers” mean any compound with an identical molecular formula but having a difference in the nature or sequence of bonding or arrangement of the atoms in space. Examples of such isomers include, for example, E and Z isomers of double bonds, enantiomers, and diastereomers. Compounds of the present invention depicting a bond with a "squiggly line" representation is intended to encompass a single is ' omer and/or both isomers of the double bond as shown below.
• Prodrug means a compound that may be converted in vivo metabolically into a compound of the present invention.
• the prodrag of a compound of the present invention may or may not have biological activity as an agonist.
• Examples of prodrags are known in the art. Examples of prodrags are provided in T. Higuchi and V. Stella, Pro-drags as Novel Delivery Systems, Vol. 14 of the A.C.S. Symposium Series; and in Edward B. Roche, ed., Bioreversible Carriers in Drug Design, American Pharmaceutical Association and Pergamon Press, 1987, both references of which are incorporated herein by reference. Prodrags may also be considered to be analogs or derivatives of the compounds of the present invention.
• the preparation of the compounds of the present invention may be performed using the standard methods know in the art of organic synthesis. Reaction transformation using compounds having functional groups may be performed on compounds with functional groups that may be protected.
• a "protected” compound or derivatives means derivatives of a compound where one or more reactive site or sites or functional groups are blocked with protecting groups. Protected derivatives are useful in the preparation of the compounds of the present invention or in themselves, the protected derivatives may be the biologically active agent.
• An example of a comprehensive text listing suitable protecting groups may be found in T.W. Greene, Protecting Groups in Organic Synthesis, 3rd edition, John Wiley & Sons, Inc. 1999.
• The- synthesis of compounds of Formulae II and III is in Scheme 1.
• the corresponding amides can be prepared as described by Nuvole, A. et al. J. Chem. Soc. Perkin Trans. 1, 1989, 1007-1011 and Dabrowski, J. et al. Tetrahedron, 1976, 32, 1025-1029.
• Scheme 1 :
• R 5 alkyl
• compound 5 can be prepared according to Collins, J. L. et al. US 6,498,174 or by using the method of Atkins, R. J., et al. Organic Process Research & Development 1997, 1, 185-197 or Popic, et al. Synthesis 1991, 195-198.
• R 5 - alkoxy
• compound 5 is prepared according to the method of Oikawa, Y. et al. J. Org. Chem. 1978, 43(10), 2087-2088.
• the resultant P 2 pellet was resuspended in ice-cold 50 mM sodium potassium phosphate (J.T. Baker) buffer (pH 7.4) containing 200 mM NaCl (J.T. Baker) and used immediately in binding assays.
• a 2nM concentration of [ 35 S]TBPS (86 Ci/mmol; New England Nuclear, Boston, MA, USA) was incubated with 100 ⁇ l of tissue homogenate (10% w/v) in the presence or absence of 5 ⁇ M GABA (Sigma Chem. Co., St. Louis, MO) and 5 ⁇ l aliquots of test drag dissolved in dimethyl sulfoxide (Sigma Chem. Co.) ( ⁇ 10 ⁇ l of solvent used in all assays).
• Electrophysiological Assay 1 Pregnant Sprague-Dawley rats, incubating embryos of 17-19 days gestation, were sacrificed by cervical dislocation. The embryos were removed under aseptic conditions and the brains quickly excised and placed in Hank's balanced salt solution (HBSS, Gibco) at ambient room temperature (18-22 °C).
• HBSS Hank's balanced salt solution
• the hippocampi were dissected out and chopped into fragments ( ⁇ 2 mm ) and transferred into an enzyme solution containing (in mM): NaCl 116, KG 5.4, NaHCO 3 26, NaH 2 PO 4 1, CaCl 2 1.5, MgSO 4 1, EDTA 0.5, glucose 25, cysteine 1, and papain 20 U/ml (Sigma) and incubated at 37 °C, 5% CO 2 , 100% relative humidity for 1 hr. Tissue fragments were washed in HBSS containing 1 mg/ml of bovine serum albumin (BSA) and 1 mg/ml of ovomucoid (both Sigma).
• BSA bovine serum albumin
• Tissue was transferred into a further 3-4 ml of this solution and gently triturated into a single cell suspension using a fire-polished Pasteur pipette.
• the single cell suspension was layered on to 5 ml HBSS containing 10 mg/ml of BSA and 10 mg/ml of ovomucoid and centrifuged at 100 X g for 10 min. The supematent was discarded and the
• the plates were maintained at 37 °C, in 5% CO 2 , and 100% relative humidity until used in electrophysiological studies. Background proliferation of non-neuronal elements was suppressed with cytosine arabinoside (10 ⁇ M, Sigma) for 48 hr 7 days after intitial dissociation.
• the compounds of the present invention that evoked membrane currents were recorded from hippocampal neurons using the whole cell configuration of the patch-clamp technique. Neurons were voltaged clamped at -60 mV using a List electronics L/M EPC-7 converter head stage and amplifier.
• the recording electrode was filled with an internal solution composed of (in mM): CsCl or KC1 140, MgCl 2 2, CaCl 2 0.1, EGTA 1.1 (free Ca 2+ ⁇ 10 "8 M), HEPES- NaOH 10, and ATP-Mg 2+ 2.
• the recording electrodes were fabricated from glasss hematocrit tubes (Kimble sodalime tubes 73811) on Narishige PB7 two stage electrode puller. Electrodes were coated within 100 ⁇ m of the tip with "Sylgard” (Dow Coming) and fire polished just before use.
• the compounds were applied locally to the soma of a voltage-clamped neuron by pressure ejection (1.4 Kpa, 10-80 msec, 0.1-0.033 Hz) from the tip of a modified recording pipette using a Picospritzer H device (General Valve Corporation).
• the compound-containing pipette was positioned within 0.1 mm of the cell using a Leitz micromanipulator.
• the microscope and micromanipulators were all mounted on a vibration-free isolation air table (Wentworth) placed inside a Faraday cage.
• the compound-evoked whole cell currents were monitored on a storage oscilloscope (Tektronix 2212), recorded, after digital pulse code modulation (frequency response 14 kHz, Sony PCM 701), and displayed on Multitrace (Electromed) pen chart recorder (frequency response 0.5 kHz). All drags, other than- the compounds of the present invention, were applied to cells via the superfusion system. Compound-evoked whole cell currents were measured at their peak. Responses in the presence of drags expressed as the arithmetic mean + SEM of responses in the absence (control) or drugs.
• Electrophysiology Assay 2 GABA A subunit transfected HEK cells are maintained at 37 °C and 5% CO 2 using Dulbecco's Modified Eagle's Medium with L-glutamine and no sodium pyruvate (Irvine Scientific #9031, Irvine CA) and supplemented with 10% fetal bovine serum (Irvine Scientific #3000), 10 U/ml hygromycin B (Calbiochem #400051), and an antibiotic cocktail consisting of 100 ⁇ g/ml streptomycin sulfate, 0.25 ⁇ g/ml amphotericin B, 100 units/ml penicillin G (Gibco 15240-096, Gaithersburg MD).
• Cells are passed by 2 X wash with phosphate buffered saline (PBS) pH 7.4 and lifted using 1 X trypsin/EDTA solution in PBS (0.5 mg/ml trypsin, 0.2 mg/ml EDTA, Irvine Scientific #9342) when confluency reaches -90%.
• PBS phosphate buffered saline
• 1 X trypsin/EDTA solution in PBS (0.5 mg/ml trypsin, 0.2 mg/ml EDTA, Irvine Scientific #9342) when confluency reaches -90%.
• GABA A subunit transfected HEK cells are grown to -70% confluency on slide. Cells are transferred to a bath that is continuosly perfused with extracellular saline.
• the extracellular medium contained 145 mM NaCl, 3 mM KC1, 1.5 mM CaCl 2 , 1 mM MgCl 2 , 5.5 mM d-glucose, and 10 mM HEPES, pH 7.4 at an osmolarity of 320-330 mosM. Recordings are performed at room temperature using the whole cell patch clamp technique.
• the patch pipette solution contained 147 mM N-methyl-D-glucamine hydrochloride, 5 mM CsCl, 5 mM K 2 ATP, 5 mM HEPES, 1 mM MgCl 2 , 0.1 mM CaCl 2 , and 1.1 mM EGTA, pH 7.2, at an osmolarity of 315 mosM.
• Pipette-to-bath resistance is typically 3-5 Mohms. Cells are voltage clamped at -60 mV, and the chloride equilibrium potential was approximately 0 mV. Drugs are dissolved in extracellular medium and rapidly applied to the cell by local perfusion. A motor driven multi- channel switching system exchanged solutions in approximately 20 ms.
• mice are injected (i.p.) with various doses of drug dissolved in DMSO or vehicle (DMSO 5 ⁇ /g body weight) at time of peak effect before administration (s.c.) of a CD 97 dose of metrazol (85 mg/kg), (+)-bicuculline (2.7 mg/kg), or picrotoxin (3.15 mg/kg), or vehicle (0.9% saline 5 l/g body weight), immediately after the injection mice are observed for a period of 45-60 minutes. The number of animals with tonic/clonic convulsions is recorded. Vogel conflict Adult male rats are randomly divided into groups of 6 rats/group. Animals were deprived of water overnight (16hr). Food was freely available at time of thirsting.
• test drug i.p.
• control drag diazepam
• vehicle control rats are placed in a square plexiglass box containing a stainless steel bottom connected to one side of a drinkometer circuit.
• a water bottle placed so the drink tube extends into the plexiglass box, is connected.
• an electric shock is delivered at the tube after seven licks are recorded.
• the number of licks in a 10 min session is recorded.
• Light-dark transition Male NSA mice (25-30g) are used.
• the apparatus consists of an open-topped box divided into small and large area by a partition that has a hole at floor level.
• the small compartment is painted black and the large compartment white.
• the white compartment was illuminated with light and the black compartment with red light.
• the time spent in the light compartment and the number of transitions between compartments are recorded during a 3 min test session.
• Vehicle or test compounds are administered 30 min prior to the test.
• Diazepam is administered (i.p.) at 2 mg/kg.
• Example 1 Ethyl 2-chloro-a-[(dimethylamino)methylene]- ⁇ -oxo-benzenepropanoate
• a mixture of ethyl 3,3-dimethylaminoacrylate (4.68 g, 32.7 mmol) and N,N- diisopropylethylamine (12 mL, 8.9 g, 69 mmol) was stirred at rt and a solution of 2- chlorobenzoyl chloride (5.72 g, 32.7 mmol) in 30 mL of toluene was added over 5 mins. The yellow solution that formed was placed in an oil bath at 85-90 °C.
• Example 3 l,l-Dimethylethyl 2-chloro- ⁇ -[[(4-iodophenyl)amino]methylene]- ⁇ -oxo-benzenepropanoate 1,1-Dimethylethyl 2-chlorobenzoylacetate.
• a solution of 5-(2-chlorobenzoyl)-2,2- dimethyl-l,3-dioxane-4,6-dione (539 mg, 1.91 mmol) in 17 mL of toluene was treated with 0.6 mL (465 mg, 6.27 mmol) of 2-methyl-2- ⁇ ropanol and heated at 80-85 °C. After 4.5 h, the reaction was allowed to cool and concentrated in vacuo.
• Example 10 l,3-Diphenyl-2-[(4-iodophenyl)amino)methylene]-l,3-propanedione 2-[(Dimethylamino)methylene]-l,3-diphenyl-l,3-propanedione: To a solution of dibenzoylmethane (1.072 g, 4.78 mmol) in 6 mL of toluene was added neat N,N- dimethylformamide dimethylacetal (0.7 mL, 630 mg, 5.25 mmol) dropwise via syringe. The resulting solution was stirred at rt for 1 h and then heated at reflux for 16 h.

Landscapes

• Organic Chemistry (AREA)
• Chemical & Material Sciences (AREA)
• Health & Medical Sciences (AREA)
• Bioinformatics & Cheminformatics (AREA)
• Engineering & Computer Science (AREA)
• Veterinary Medicine (AREA)
• Biomedical Technology (AREA)
• Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
• General Chemical & Material Sciences (AREA)
• Pharmacology & Pharmacy (AREA)
• Life Sciences & Earth Sciences (AREA)
• Animal Behavior & Ethology (AREA)
• General Health & Medical Sciences (AREA)
• Public Health (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Neurosurgery (AREA)
• Medicinal Chemistry (AREA)
• Neurology (AREA)
• Psychiatry (AREA)
• Pain & Pain Management (AREA)
• Addiction (AREA)
• Anesthesiology (AREA)
• Hospice & Palliative Care (AREA)
• Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
• Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
• Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
• Nitrogen Condensed Heterocyclic Rings (AREA)
• Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

Priority Applications (9)

Applications Claiming Priority (2)

Publications (2)

Family

ID=35320783

Family Applications (1)

Country Status (14)

Cited By (8)

Families Citing this family (2)

Citations (1)

Family Cites Families (9)

• 2005
  • 2005-05-05 MX MXPA06012839A patent/MXPA06012839A/es unknown
  • 2005-05-05 US US11/123,597 patent/US7825278B2/en not_active Expired - Fee Related
  • 2005-05-05 CA CA002565627A patent/CA2565627A1/en not_active Abandoned
  • 2005-05-05 WO PCT/US2005/015869 patent/WO2005108347A2/en active Application Filing
  • 2005-05-05 JP JP2007511639A patent/JP5002452B2/ja not_active Expired - Fee Related
  • 2005-05-05 RU RU2006142896/04A patent/RU2006142896A/ru not_active Application Discontinuation
  • 2005-05-05 UA UAA200612755A patent/UA85711C2/ru unknown
  • 2005-05-05 ZA ZA200609924A patent/ZA200609924B/xx unknown
  • 2005-05-05 CN CNA2005800214141A patent/CN1976892A/zh active Pending
  • 2005-05-05 EP EP05750643A patent/EP1742904B1/en not_active Not-in-force
  • 2005-05-05 BR BRPI0510715-6A patent/BRPI0510715A/pt not_active IP Right Cessation
  • 2005-05-05 AU AU2005240657A patent/AU2005240657A1/en not_active Abandoned
• 2006
  • 2006-11-06 IL IL179068A patent/IL179068A0/en unknown
  • 2006-12-05 NO NO20065595A patent/NO20065595L/no not_active Application Discontinuation

Patent Citations (1)

Non-Patent Citations (6)

Also Published As

Similar Documents

Legal Events